☆ 3.8 Review

Autoimmune diseases and cancers overlapping with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD): A systematic review

MULTIPLE SCLEROSIS JOURNAL-EXPERIMENTAL TRANSLATIONAL AND CLINICAL (2022)

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Article Clinical Neurology

Clinico-radiological characteristics of anti-myelin oligodendrocyte glycoprotein antibody-associated autoimmune encephalitis in children

Ji Yeon Han et al.

Summary: This study investigated the clinical characteristics and prevalence of paediatric anti-MOG antibody-associated autoimmune encephalitis. The results showed that anti-MOG antibody-associated encephalitis accounts for a significant proportion of paediatric patients with autoimmune encephalitis. Patients with this disease had a favorable response to immunotherapy.

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2022)

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Article Clinical Neurology

Clinical analysis of myelin oligodendrocyte glycoprotein antibody-associated demyelination in children: A single-center cohort study in China

Xin Wang et al.

Summary: The clinical phenotypes of MOGAD are age-dependent, with younger onset ages for ADEM compared to ON children. The cerebral lesions are diverse and can manifest as ADEM-like, leukodystrophy-like, ON, and other patterns. The titers of MOG-Ab should not be the sole basis for recurrence and long-term treatment. Most children have a good prognosis, but ADEM-ON phenotype tends to relapse, sometimes leading to cognitive impairment, epilepsy, and other sequelae. Repeated ON can cause visual impairment.

MULTIPLE SCLEROSIS AND RELATED DISORDERS (2022)

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Letter Clinical Neurology

Pediatric anti-N-methyl-D-aspartate receptor encephalitis with MOG-Ab co-existence: Relapse propensity and treatability

Zhang Weihua et al.

Summary: This study investigated the clinical characteristics of pediatric patients with anti-NMDAR encephalitis and positive MOG-Ab, finding that patients with both antibodies are more prone to relapse. Long-term treatment with disease-modifying drugs can significantly reduce the annualized relapse rates in these patients.

MULTIPLE SCLEROSIS AND RELATED DISORDERS (2022)

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Review Neurosciences

Relapsing MOG-IgG-associated diseases coexisting with anti-NMDAR encephalitis: a case report and literature review

Mengmeng Wang et al.

Summary: This article reports a rare case of MNOS and summarizes the clinical characteristics, diagnosis, and treatment of MNOS in adults through literature review. The results showed that MNOS has diverse clinical manifestations, immunotherapy is the primary treatment, and MNOS tends to relapse, requiring monitoring of relevant markers.

JOURNAL OF INTEGRATIVE NEUROSCIENCE (2022)

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Article Immunology

Case Report: A Case With MOGAD and Anti-NMDAR Encephalitis Overlapping Syndrome Mimicing Radiological Characteristics of CLIPPERS

Jia Guo et al.

Summary: This article reports a rare case of antibody overlap syndrome that mimicked CLIPPERS on imaging but was ultimately diagnosed as MNOS, with symptom relief after treatment. Future research should focus more on the diagnosis and treatment of such diseases.

FRONTIERS IN IMMUNOLOGY (2022)

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Article Clinical Neurology

Clinical Profile and Treatment Outcome in MOGAD: A Single-Center Case-Series Study in Guiyang, China

Xiaoyang Lei et al.

Summary: The clinical spectrum of MOGAD is diverse, with presentations including APS and CLIPPERS-form. Most patients received methylprednisolone treatment and showed favorable long-term outcomes. Further research is needed to determine risk factors for relapse and identify optimal steroid-sparing agents.

FRONTIERS IN NEUROLOGY (2022)

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Letter Radiology, Nuclear Medicine & Medical Imaging

Rare autoimmune encephalitis presenting as fluid-attenuated inversion recovery-hyperintense lesions in anti-Myelin oligodendrocyte glycoprotein-associated encephalitis and seizures accompanied with anti-IgLON5 antibody

Wanyao Li et al.

QUANTITATIVE IMAGING IN MEDICINE AND SURGERY (2022)

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Overlapping syndrome of recurrent anti-N-methyl-D-aspartate receptor encephalitis and anti-myelin oligodendrocyte glycoprotein demyelinating diseases: A case report

Xue-Jing Yin et al.

Summary: We report a rare case of overlap syndrome with anti-NMDA receptor encephalitis and anti-myelin oligodendrocyte glycoprotein antibody disease. This emphasizes the rarity of this antibody combination and suggests the need for longer follow-up in these patients due to the risk of recurrence of two autoimmune disorders.

WORLD JOURNAL OF CLINICAL CASES (2022)

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Coexistent anti-GFAP and anti-MOG antibodies presenting with isolated meningitis and papillitis: more support for overlapping pathophysiology

Andrew J. Martin et al.

Summary: This case of overlapping anti-GFAP and anti-MOG antibody-associated syndrome expands the phenotype and provides insights into the pathophysiology of each condition.

BMJ NEUROLOGY OPEN (2022)

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Editorial Material Clinical Neurology

Sjogren Disease and Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis

Aman Mittal et al.

JOURNAL OF NEURO-OPHTHALMOLOGY (2021)

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Article Clinical Neurology

Comparative study of AQP4 antibody-related diseases and MOG antibody-related diseases among the population in Hunan, China

Xiqian Chen et al.

Summary: AQP4 antibody-positive patients have a higher prevalence in women, are more likely to have spinal cord involvement symptoms and connective tissue antibody abnormalities, and usually exhibit more severe clinical symptoms and residual neurological deficits after treatment than MOG antibody-positive patients.

ACTA NEUROLOGICA BELGICA (2021)

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Article Clinical Neurology

Coexisting systemic and organ-specific autoimmunity in MOG-IgG1-associated disorders versus AQP4-IgG+ NMOSD

Amy Kunchok et al.

Summary: MOG-IgG1-associated disorders are not strongly associated with non-organ and organ-specific autoantibodies, while AQP4-IgG+ NMOSD is significantly associated with systemic lupus erythematous (SLE), indicating differences in co-existing systemic and organ-specific autoimmunity between the two conditions.

MULTIPLE SCLEROSIS JOURNAL (2021)

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Article Neurosciences

Evaluation of diagnostic criteria and red flags of myelin oligodendrocyte glycoprotein encephalomyelitis in a clinical routine cohort

Krenar Veselaj et al.

Summary: Evaluating diagnostic and red flag criteria, MOG-IgG retesting (including changing assays), and CSF-specific OCB are crucial in clinical routine cohorts for distinguishing MOG-EM from MS. The presence of red flags should be considered when diagnosing possible MOG-EM in patients with borderline MOG-IgG.

CNS NEUROSCIENCE & THERAPEUTICS (2021)

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Video-Polysomnographic Assessment for the Diagnosis of Disorders of Arousal in Children

Regis Lopez et al.

Summary: This study highlights the importance of SWS fragmentation and slow/mixed arousal indexes as biomarkers for the diagnosis of DOA in children, with different cutoff values obtained than those validated in adults. The study provides Class III evidence that these parameters accurately identify children with DOA.

NEUROLOGY (2021)

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Antibody prevalence and immunotherapy response in Chinese patients with epilepsy and encephalopathy scores for patients with different neuronal surface antibodies

Yu Jia et al.

Summary: The study evaluated the application of antibody prevalence and response to immunotherapy in Chinese patients with epilepsy and encephalopathy, finding that APE2-CHN had the highest value for predicting the positivity of NMDAR-Ab. Additionally, RITE2-CHN appropriately evaluated the response of immunotherapy for anti-LGI1 encephalitis. However, RITE2 and RITE2-CHN did not appear to be good predictors of immunotherapy outcomes for patients with specific neuronal-surface antibodies, and high APE2-CHN scores often indicated a poor response to immunotherapy.

CHINESE MEDICAL JOURNAL (2021)

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Clinical analysis of a patient simultaneously positive for antibodies of myelin oligodendrocyte glycoprotein and anti-N-methyl-D-aspartate receptor A case report

Liming Cao et al.

Summary: The co-occurrence of MOG-Ab and anti-NMDAR-Ab does not indicate overlapping MOG-AD and anti-NMDARe. Laboratory findings should be combined with clinical features for an accurate diagnosis.

MEDICINE (2021)

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Review Clinical Neurology

Clinical features and management of coexisting anti-N-methyl-D-aspartate receptor encephalitis and myelin oligodendrocyte glycoprotein antibody-associated encephalomyelitis: a case report and review of the literature

Di Nan et al.

Summary: The study analyzed 25 patients with coexisting anti-NMDA receptor encephalitis and MOG antibody-associated encephalomyelitis. Treatment with intravenous methylprednisolone and immunoglobulin was most commonly used, with second-line treatments leading to good outcomes. Clinical symptoms such as seizures and cognitive decline along with atypical central nervous system demyelination can serve as warning signs for possible dual diagnosis.

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Anti-NMDAR encephalitis may develop concurrently with anti-MOG antibody-associated bilateral medial frontal cerebral cortical encephalitis and relapse with elevated CSF IL-6 and CXCL13

Juichi Fujimori et al.

Summary: In this study, a patient with relapsing anti-NMDAR encephalitis was found to be double positive for anti-NMDAR and anti-MOG antibodies at onset, with elevated levels of CSF cytokines. This suggests a possible concurrent development of NMDAR encephalitis with anti-MOG antibody-associated cortical encephalitis and relapse.

MULTIPLE SCLEROSIS AND RELATED DISORDERS (2021)

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Myelin Oligodendrocyte Glycoprotein (MOG) Antibody Positive Patients in a Multi-Ethnic Canadian Cohort

Helen Cross et al.

Summary: This study describes a multi-ethnic population with MOG antibody positivity, predominantly presenting with optic neuritis and myelitis. The median age of onset was 29 years, with a good response to steroid therapy in most patients but a high risk of relapse. Patients showed abnormalities in brain imaging, including cortical lesions and optic nerve involvement, which are common in MOG antibody-associated disease.

FRONTIERS IN NEUROLOGY (2021)

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Article Clinical Neurology

Overlapping central and peripheral nervous system syndromes in MOG antibody-associated disorders

Simon Rinaldi et al.

Summary: Antibodies to myelin oligodendrocyte glycoprotein (MOG) are associated with CNS demyelination including optic neuritis and transverse myelitis. The study of an Australasian MOGAD cohort revealed a subgroup possibly mediated by coexistent autoantibodies, presenting with myeloradiculitis, combined central and peripheral demyelination syndromes, and inflammatory neuropathies, being responsive to immunotherapy.

NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION (2021)

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Evidence for and against subclinical disease activity and progressive disease in MOG antibody disease and neuromyelitis optica spectrum disorder

Negar Molazadeh et al.

Summary: MOGAD and AQP4-IgG+ NMOSD are generally relapsing disorders with potential for prolonged periods of remission, unlike multiple sclerosis. Recent studies have explored evidence for progressive disease courses in these conditions.

JOURNAL OF NEUROIMMUNOLOGY (2021)

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Letter Clinical Neurology

Myelin oligodendrocyte glycoprotein antibody-associated disorders coexisting with ankylosing spondylitis: Potential association between demyelination and tumor necrosis factor inhibitors

Wenjng Luo et al.

Summary: MOGAD is a newly described demyelinating disease, which may have potential associations with AS and TNFα inhibitors. Further studies are needed to clarify the risk of demyelinating events following anti-TNFα therapy and to elucidate the relationship between MOGAD and AS.

MULTIPLE SCLEROSIS AND RELATED DISORDERS (2021)

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Letter Clinical Neurology

FLAIR-hyperintense lesions in anti-MOG-associated encephalitis with seizures (FLAMES) unmasked by withdrawal of immunosuppression for Crohn's disease?

Svetlana Stamenova et al.

Summary: A 31-year-old pregnant woman presented with headache, fever, and seizures, which were diagnosed as cortical FLAIR-hyperintense lesions in Anti-MOG-associated Encephalitis with seizures (FLAMES). Extensive testing did not reveal any infectious, autoimmune, or malignant causes of the encephalitis.

MULTIPLE SCLEROSIS AND RELATED DISORDERS (2021)

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Article Clinical Neurology

Case Report: Anti-NMDAR Encephalitis With Anti-MOG CNS Demyelination After Recurrent CNS Demyelination

Bing-Yan Ren et al.

Summary: This case report presents a patient with anti-NMDAR encephalitis combined with anti-MOG CNS demyelination following recurrent CNS demyelination. Repeat autoantibodies testing in CSF/serum assisted in making an early definite diagnosis. Treatment with MMF and corticosteroid resulted in good therapeutic effects.

FRONTIERS IN NEUROLOGY (2021)

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Review Clinical Neurology

Neuromyelitis optica spectrum disorder (NMOSD) associated with cancer: A systematic review

Sareh Shahmohammadi et al.

Summary: NMOSD is closely associated with cancer, especially in older patients. Screening for lung, breast, and genitourinary cancers is recommended for NMOSD patients, and cancer resection has a positive impact on treatment and recovery of NMOSD.

MULTIPLE SCLEROSIS AND RELATED DISORDERS (2021)

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Clinical and Imaging Features of Patients With Encephalitic Symptoms and Myelin Oligodendrocyte Glycoprotein Antibodies

Jingsi Wang et al.

Summary: The study describes the clinical and imaging features of patients with MOG-E in a medical center. Most patients had acute or subacute onset of encephalitic symptoms. MRI abnormalities were observed in all patients, with the most common lesion locations being cortical/subcortical, deep/periventricular white matter, and corpus callosum. The study suggests that chronically progressive encephalitis may be a new phenotype of MOGAD, and recommends testing for MOG-ab in subacute and chronic progressive dementia with leukodystrophy-like MRI lesions.

FRONTIERS IN IMMUNOLOGY (2021)

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Article Immunology

Clinical and Radiological Characteristics of Children and Adults With First-Attack Myelin Oligodendrocyte Glycoprotein Antibody Disease and Analysis of Risk Factors for Predicting the Severity at Disease Onset in Central China

Yanfei Li et al.

Summary: The study revealed differences in clinical presentation of MOGAD in patients of different ages, with risk factors for higher initial EDSS scores mainly related to levels of uric acid and Hcy.

FRONTIERS IN IMMUNOLOGY (2021)

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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy in Children: A Retrospective Analysis of 35 Cases

Hongjun Fang et al.

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FRONTIERS IN IMMUNOLOGY (2021)

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Identification of the clinical and neuroimaging characteristics in children with neuromyelitis optica spectrum disorders: a case series

Zhan Zhang et al.

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Positive Predictive Value of Myelin Oligodendrocyte Glycoprotein Autoantibody Testing

Elia Sechi et al.

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JAMA NEUROLOGY (2021)

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Overlapping syndrome of anti-N-methyl-D-aspartate receptor encephalitis and anti-myelin oligodendrocyte glycoprotein inflammatory demyelinating diseases: A distinct clinical entity?

Weibi Chen et al.

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MULTIPLE SCLEROSIS AND RELATED DISORDERS (2021)

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Opsoclonus myoclonus syndrome in a postpartum period

Srijan Adhikari et al.

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MULTIPLE SCLEROSIS AND RELATED DISORDERS (2021)

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Overlapping syndrome mimicking infectious meningoencephalitis in a patient with MOG and GFAP IgG

Suqiong Ji et al.

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BMC NEUROLOGY (2021)

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David Weiss et al.

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BMC PSYCHIATRY (2021)

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Autoimmune neurology: Co-occurrence of anti-NMDAR encephalitis and anti-MOG associated disease, report of a case

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Myelin-oligodendrocyte glycoprotein antibody-associated disease

Romain Marignier et al.

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Article Clinical Neurology

Co-occurrence of Anti-N-Methyl-D-Aspartate Receptor Encephalitis and Anti-myelin Oligodendrocyte Glycoprotein Inflammatory Demyelinating Diseases: A Clinical Phenomenon to Be Taken Seriously

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Overlapping demyelinating syndrome and anti-N-methyl-D-aspartate receptor encephalitis with seizures

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EPILEPSY & BEHAVIOR REPORTS (2019)

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Article Rheumatology

Positive anti-MOG antibodies in a patient with Sjogren's syndrome and transverse myelitis

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EUROPEAN JOURNAL OF RHEUMATOLOGY (2019)

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Article Clinical Neurology

Clinical characteristics of myelin oligodendrocyte glycoprotein seropositive optic neuritis: a cohort study in Shanghai, China

Guixian Zhao et al.

JOURNAL OF NEUROLOGY (2018)

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Article Clinical Neurology

Clinical course, therapeutic responses and outcomes in relapsing MOG antibody-associated demyelination

Sudarshini Ramanathan et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2018)

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Article Clinical Neurology

MOG Spectrum Disorders and Role of MOG-Antibodies in Clinical Practice

Eva-Maria Hennes et al.

NEUROPEDIATRICS (2018)

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Article Clinical Neurology

Autoimmune Encephalitis Epidemiology and a Comparison to Infectious Encephalitis

Divyanshu Dubey et al.

ANNALS OF NEUROLOGY (2018)

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Article Immunology

An unusual case of anti-MOG CNS demyelination with concomitant mild anti-NMDAR encephalitis

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JOURNAL OF NEUROIMMUNOLOGY (2018)

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Article Rheumatology

Understanding the Antibody Repertoire in Neuropsychiatric Systemic Lupus Erythematosus and Neuromyelitis Optica Spectrum Disorder

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ARTHRITIS & RHEUMATOLOGY (2018)

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Article Clinical Neurology

Comparison of myelin oligodendrocyte glycoprotein (MOG)-antibody disease and AQP4-IgG-positive neuromyelitis optica spectrum disorder (NMOSD) when they co-exist with anti-NMDA (N-methyl-D-aspartate) receptor encephalitis

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MULTIPLE SCLEROSIS AND RELATED DISORDERS (2018)

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Article Clinical Neurology

Autoimmune and immunogenetic profile of patients with optic neuritis in a population-based cohort

K. Soelberg et al.

MULTIPLE SCLEROSIS AND RELATED DISORDERS (2018)

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Article Clinical Neurology

Overlapping Autoimmune Syndromes in Patients With Glial Fibrillary Acidic Protein Antibodies

Xinguang Yang et al.

FRONTIERS IN NEUROLOGY (2018)

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Article Clinical Neurology

NMOSD with anti-MOG antibodies following anti-TNFα therapy: A case report

Emilie Lommers et al.

MULTIPLE SCLEROSIS AND RELATED DISORDERS (2018)

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Article Clinical Neurology

Risk factors for mortality in patients with anti-NMDA receptor encephalitis

X. Chi et al.

ACTA NEUROLOGICA SCANDINAVICA (2017)

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Article Clinical Neurology

Cerebrospinal fluid levels of neurofilament and tau correlate with brain atrophy in natalizumab-treated multiple sclerosis

J. Mellergard et al.

EUROPEAN JOURNAL OF NEUROLOGY (2017)

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Article Clinical Neurology

Hashimoto's encephalopathy and anti-MOG antibody encephalitis: 50 years after Lord Brain's description

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EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY (2017)

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Article Clinical Neurology

Poster Session 1

Multiple Sclerosis Journal (2017)

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Article Clinical Neurology

Poster Session 1

Multiple Sclerosis Journal (2017)

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Article Clinical Neurology

Cerebral cortical encephalitis followed by recurrent CNS demyelination in a patient with concomitant anti-MOG and anti-NMDA receptor antibodies

Lei Zhou et al.

MULTIPLE SCLEROSIS AND RELATED DISORDERS (2017)

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Article Rheumatology

Autoantibodies against myelin sheath and S100β are associated with cognitive dysfunction in patients with rheumatoid arthritis

Talita Siara Almeida Baptista et al.

CLINICAL RHEUMATOLOGY (2017)

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Article Clinical Neurology

Antibodies to myelin oligodendrocyte glycoprotein in aquaporin 4 antibody seronegative longitudinally extensive transverse myelitis: Clinical and prognostic implications

Alvaro Cobo-Calvo et al.

MULTIPLE SCLEROSIS JOURNAL (2016)

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Article Clinical Neurology

Antibodies to myelin oligodendrocyte glycoprotein in aquaporin 4 antibody seronegative longitudinally extensive transverse myelitis: Clinical and prognostic implications

Alvaro Cobo-Calvo et al.

MULTIPLE SCLEROSIS JOURNAL (2016)

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Article Clinical Neurology

Paediatric brainstem encephalitis associated with glial and neuronal autoantibodies

Yael Hacohen et al.

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2016)

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Article Immunology

Age exacerbates the CCR2/5-mediated neuroinflammatory response to traumatic brain injury

Josh M. Morganti et al.

JOURNAL OF NEUROINFLAMMATION (2016)

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Letter Pediatrics

Anti-myelin oligodendrocyte glycoprotein antibody neuritis optica following anti-NMDA receptor encephalitis

Koji Yokoyama et al.

PEDIATRICS INTERNATIONAL (2016)

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Article Biology

Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD

Yaping Yan et al.

SCIENCE CHINA-LIFE SCIENCES (2016)

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Article Clinical Neurology

Pactrims Invited Lecture / Ordinary Submission

Multiple Sclerosis Journal (2015)

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Article Clinical Neurology

Clinical Profile of Anti-Myelin Oligodendrocyte Glycoprotein Antibody Seropositive Cases of Optic Neuritis

Ryusaku Matsuda et al.

NEURO-OPHTHALMOLOGY (2015)

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Article Clinical Neurology

Antibodies to Aquaporin 4, Myelin-Oligodendrocyte Glycoprotein, and the Glycine Receptor α1 Subunit in Patients With Isolated Optic Neuritis

Eugenia Martinez-Hernandez et al.

JAMA NEUROLOGY (2015)

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Article Clinical Neurology

Pactrims Invited Lecture / Ordinary Submission

Multiple Sclerosis Journal (2015)

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Article Clinical Neurology

Antibodies to MOG and AQP4 in adults with neuromyelitis optica and suspected limited forms of the disease

Romana Hoeftberger et al.

MULTIPLE SCLEROSIS JOURNAL (2015)

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Article Clinical Neurology

Fulminant demyelinating encephalomyelitis Insights from antibody studies and neuropathology

Franziska Di Pauli et al.

NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION (2015)

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Article Clinical Neurology

MOG cell-based assay detects non-MS patients with inflammatory neurologic disease

Patrick Waters et al.

NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION (2015)

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Article Clinical Neurology

Overlapping demyelinating syndromes and anti-N-methyl-D-aspartate receptor encephalitis

Maarten J. Titulaer et al.

ANNALS OF NEUROLOGY (2014)

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Article Clinical Neurology

Distinction between MOG antibody-positive and AQP4 antibody-positive NMO spectrum disorders

Douglas Kazutoshi Sato et al.

NEUROLOGY (2014)

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Article Clinical Neurology

Neuromyelitis Optica Spectrum Disorders With Aquaporin-4 and Myelin-Oligodendrocyte Glycoprotein Antibodies A Comparative Study

Joanna Kitley et al.

JAMA NEUROLOGY (2014)

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Article Clinical Neurology

NMDA receptor antibodies associated with distinct white matter syndromes

Yael Hacohen et al.

NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION (2014)

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Article Clinical Neurology

Glycine receptor and myelin oligodendrocyte glycoprotein antibodies in Turkish patients with neuromyelitis optica

Mark Woodhall et al.

JOURNAL OF THE NEUROLOGICAL SCIENCES (2013)

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Article Clinical Neurology

Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study

Maarten J. Titulaer et al.

LANCET NEUROLOGY (2013)

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Article Clinical Neurology

Relationship Between NMO-Antibody and Anti-MOG Antibody in Optic Neuritis

Takeshi Kezuka et al.

JOURNAL OF NEURO-OPHTHALMOLOGY (2012)

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Article Clinical Neurology

Successful treatment of a woman with relapsing neuromyelitis optica by interferon beta

Yan Xu et al.

NEUROLOGICAL SCIENCES (2012)

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Article Immunology

Complement activating antibodies to myelin oligodendrocyte glycoprotein in neuromyelitis optica and related disorders

Simone Mader et al.

JOURNAL OF NEUROINFLAMMATION (2011)

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Article Clinical Neurology

Anti-myelin antibodies predict the clinical outcome after a first episode suggestive of MS

V. Tomassini et al.

MULTIPLE SCLEROSIS JOURNAL (2007)

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Article Clinical Neurology

Antimyelin antibodies and the risk of relapse in patients with a primary demyelinating event

S Rauer et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2006)

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